US4981518A - Bonded composite structure and method of making - Google Patents
Bonded composite structure and method of making Download PDFInfo
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- US4981518A US4981518A US07/110,615 US11061587A US4981518A US 4981518 A US4981518 A US 4981518A US 11061587 A US11061587 A US 11061587A US 4981518 A US4981518 A US 4981518A
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- fibrous cellulose
- metal oxide
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- 239000002131 composite material Substances 0.000 title claims abstract description 18
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 42
- 239000011230 binding agent Substances 0.000 claims abstract description 36
- 239000001913 cellulose Substances 0.000 claims abstract description 34
- 229920002678 cellulose Polymers 0.000 claims abstract description 34
- 239000000463 material Substances 0.000 claims abstract description 34
- 239000002253 acid Substances 0.000 claims abstract description 28
- 239000010953 base metal Substances 0.000 claims abstract description 19
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 18
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 17
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims abstract description 4
- 239000002184 metal Substances 0.000 claims abstract description 4
- 238000009877 rendering Methods 0.000 claims abstract 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 239000002245 particle Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 239000000395 magnesium oxide Substances 0.000 claims description 14
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims description 11
- 238000009413 insulation Methods 0.000 claims description 8
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 239000002699 waste material Substances 0.000 claims description 7
- 239000004014 plasticizer Substances 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 4
- 239000010902 straw Substances 0.000 claims description 4
- 239000002023 wood Substances 0.000 claims description 4
- 241000609240 Ambelania acida Species 0.000 claims description 3
- 239000010905 bagasse Substances 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 239000004114 Ammonium polyphosphate Substances 0.000 claims 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims 1
- 229920001276 ammonium polyphosphate Polymers 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 230000001473 noxious effect Effects 0.000 claims 1
- 239000007787 solid Substances 0.000 abstract description 4
- 239000002002 slurry Substances 0.000 abstract description 2
- 239000000945 filler Substances 0.000 description 12
- 239000011449 brick Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 8
- 239000004033 plastic Substances 0.000 description 8
- 229920003023 plastic Polymers 0.000 description 8
- 230000003247 decreasing effect Effects 0.000 description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- 239000004254 Ammonium phosphate Substances 0.000 description 3
- 239000003929 acidic solution Substances 0.000 description 3
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 3
- 235000019289 ammonium phosphates Nutrition 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 3
- 239000003209 petroleum derivative Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 2
- 239000004137 magnesium phosphate Substances 0.000 description 2
- 229960002261 magnesium phosphate Drugs 0.000 description 2
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 2
- 235000010994 magnesium phosphates Nutrition 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000002341 toxic gas Substances 0.000 description 2
- 229910017119 AlPO Inorganic materials 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000009435 building construction Methods 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011093 chipboard Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/34—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing cold phosphate binders
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/0076—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials characterised by the grain distribution
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/0076—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials characterised by the grain distribution
- C04B20/008—Micro- or nanosized fillers, e.g. micronised fillers with particle size smaller than that of the hydraulic binder
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B22/00—Use of inorganic materials as active ingredients for mortars, concrete or artificial stone, e.g. accelerators or shrinkage compensating agents
- C04B22/002—Water
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00034—Physico-chemical characteristics of the mixtures
- C04B2111/00129—Extrudable mixtures
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00034—Physico-chemical characteristics of the mixtures
- C04B2111/00146—Sprayable or pumpable mixtures
- C04B2111/00155—Sprayable, i.e. concrete-like, materials able to be shaped by spraying instead of by casting, e.g. gunite
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/20—Resistance against chemical, physical or biological attack
- C04B2111/28—Fire resistance, i.e. materials resistant to accidental fires or high temperatures
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Definitions
- This invention relates generally to bonded composite structures and methods for making the same. More particularly, this invention relates to bonded composite structures for forming fire resistive and insulating building materials and/or components such as panel structures, pipe insulation, and sprays for forming fire protective and insulating type coatings on pre-existing structures.
- foamed plastics could be used in buildings if they were totally encapsulated within fire resistive, nontoxic materials. Such materials were formed by encapsulating the foamed plastics in a variety of inorganic products such as a rigid homogenous foamed glass product manufactured by Pittsburgh Corning Corporation and marketed under the trademark "FOAMGLAS".
- the U.S. Pat. No. 4,419,133 to Shubow et al discloses a bonded aggregate structure for making moldable rigid insulation.
- the Shubow et al patent discloses a bonded aggregate structure made from a mixture of magnesium oxide, aluminum oxide, aggregate, and mono aluminum phosphate acidic solution.
- the aggregates disclosed are cellular, low density aggregates selected from the group including inorganic materials such as glass beads, perlite, vermiculite, and stone or other refractory aggregates.
- bonded composite structures at lower costs. Such structures must be of low cost but must also withstand high temperatures.
- the instant invention provides a low cost bonded composite structure wherein the binders are blended or mixed with a fibrous cellulose filler which is essentially a waste product that produces results similar to those achieved with the use of inorganic, insulating-type aggregates but at a much lower cost.
- a fibrous cellulose filler which is essentially a waste product that produces results similar to those achieved with the use of inorganic, insulating-type aggregates but at a much lower cost.
- Such organic materials would normally be highly flammable.
- such cellulose filler materials do not burn and form rigid bonded structures able to withstand temperatures in excess of 3000° F.
- the subject invention provides a bonded composite structure essentially consisting of a binder made from a mixture of a weak acid and a powdered base metal oxide, the acid and metal fusing as a mixture under an exothermic reaction into the binder.
- the invention is characterized by including a cellulose filler material encapsulated within the binder and rendered non-flammable thereby.
- the subject invention further provides a method of making a bonded composite structure including the steps of mixing a weak acid and a powdered base metal oxide which fuse as a mixture under an exothermic reaction into a binder.
- a cellulose filler material is encapsulated within the binder and the cellulose filler material is rendered non-flammable thereby.
- the mixture is formed into a predetermined form and the formed mixture is set and cures to a solid structure.
- the invention is a bonded composite structure consisting essentially of a binder material made from a mixture of a weak acid and a powdered base metal oxide and a cellulose filler material.
- the reaction of the acid and base metal oxide form the binder which acts as a glue for encapsulating the cellulose filler material and for adhering the bonded composite structure to whatever surface the bonded composite structure is applied.
- the bonded composite structure is made by combining three or more ingredients in varying proportions depending upon the end product and time of set desired.
- the basic ingredients include a liquid not unlike the consistency of water, a powder not unlike the consistency of Portland cement, and a cellulose filler material.
- the cellulose filler material can be selected from the group of cellulose waste materials including, but not limited to, saw dust, wood chips, shredded newspaper, straw, and bagasse. Other cellulose containing waste materials commonly discarded by the public may be utilized in the invention. The cost efficiency of these materials as compared to previously used inorganic aggregates is significant and thereby provides a distinct advantage to the subject invention. Such cellulose waste products are normally easily ignitable under normal conditions. Pursuant to the subject invention, however, the cellulose filler materials are encapsulated within the binder and rendered non-flammable thereby.
- foamed plastic insulations polystyrene, polyurenthane, isocyanrate and the like
- foamed plastic insulations can be fabricated into similar type products, they can melt at relatively low temperatures, they can burn, they can degrade under ultraviolet light, they can give off profuse amounts of smoke and toxic gases when ignited or, in some cases, only heated and, when utilized in habitable spaces, they must be enclosed or encapsulated within fire resistive materials.
- the subject invention will not begin to melt until temperatures in excess of 3000° F. have been reached. The subject invention will not burn. It will not degrade under ultraviolet light. It will not give off toxic gases, and it does not require a separate fire barrier.
- the subject invention is a fire barrier by itself.
- the foam plastic products are derivatives of petroleum and totally dependent upon the availability and price deviations of petroleum products, the subject invention is completely independent of the oil industry.
- the cellulose filler materials have a low density in the range from 3 to 15 pounds per cubic foot. Such low density materials are preferred in applications where high mass is a problem and low weight is desired.
- the weak acid is selected from the group including mono aluminum phosphate.
- Other weak acids may be used which in combination with the powdered base metal oxide, such as magnesium oxide, form a magnesium phosphate solid.
- Such a magnesium phosphate solid will normally be formed relative quickly and stick to almost anything and binds together whatever materials might also happen to be in contact with the mixture.
- the weak acid and base metal oxide may be combined in a range of ratios from “3 to 1" to "1 to 3", respectively by weight.
- the cellulose filler materials are combined with the weak acid in a "1 to 1" to "1 to 6" ratio by weight.
- the binder has a predetermined setting time.
- the binder can include water and/or other ingredient similar to those disclosed in the Shubow patent for delaying the setting time, the amount of water by part being directly related to the setting time.
- the set is chemical as when concrete or plaster mixes set. This is not a cure in the technical sense. Increasing the water content of the mixture can increase the setting time from an instantaneous to a 10 minute set.
- Aluminum oxide can also be added to the mixture to increase the setting time. Increasing the relative proportion of aluminum oxide increases the setting time.
- the weight ratio of aluminum oxide to acidic solution is from about 1:1 to about 1:3 and the weight ratio of magnesium oxide to aluminum oxide is from about 1:1 to about 1:6.
- Plasticizers can be used to adjust the plasticity of the final product without the further addition of water. Alternatively, plasticity can be kept constant by decreasing the amount of water in the mixture and adding a plasticizer.
- An example of a plasticizer is polypyrogenic silica having a particle size of 0.01 to 0.02 microns or the equivalent sold as X-59TM manufactured by Cabot Corporation, Boston, Mass.
- the base metal can be magnesium oxide purchased from Martin Marietta Chemicals under the trade name MegChem.
- the base metal may include powder particles of a predetermined extent of being finally divided, the extent of being finally divided of the powder particles is directly related to the setting time.
- the magnesium oxide may be purchased from Martin Marietta Chemicals as MagChem 40 or MagChem 30.
- MagChem 40 typically includes 98% magnesium oxide, has a particle size of 5 microns, and a surface area of 45 gm 2 .
- MagChem 30 is typically 98% magnesium oxide, has a particle size of 5 microns and a surface area of 20 gm 2 .
- the setting time for MagChem 30 is slower than the setting time for MagChem 40. This is attributed to MagChem 40 having more surface area.
- the ammonium phosphate or aluminum phosphate may be purchased as ammonium phosphate or aluminum phosphate solution from Stauffer Chemical Company.
- Aluminum phosphate solution may also be referred to as aluminum phosphate or an acidic solution of mono aluminum phosphate.
- the ammonium phosphate or aluminum phosphate are a clear water white acidic aqueous solutions and are generally purchased as a 50% aqueous solutions.
- the subject invention further provides a method of making the bonded composite structure.
- the method includes the steps of mixing the acid and the powdered base metal oxide which fuse as a mixture under an exothermic reaction into a binder.
- the fibrous cellulose material is encapsulated within the binder and is rendered non-flammable thereby.
- the mixture is formed into a predetermined form and the predetermined form is set during a predetermined period of time.
- the time for setting may be instantaneous or range up to or greater than 10 minutes.
- the setting time may be controlled by various factors set forth below. The setting time is chosen based on the desired end use of the encapsulated composite material.
- the mixture may be formed by extruding the mixture to form pipe insulation.
- water may be added to the mixture to delay the setting step for 30 second to 1 minute.
- Such alternation of the mixture provides what would be considered an intermediate setting time in comparison to the normally instantaneous setting time of the mixture.
- a less finally divided powdered metal oxide can be used to delay the setting step for 30 second to 1 minute.
- the forming step may alternatively take the form of spraying the mixture onto a previously existing structure to form a fire protective and/or insulation layer on the structure. It is preferable in a spraying step to have material which almost instantaneously sets in 1 to 2 seconds.
- a blending approach wherein the three ingredients are mixed together provides an almost immediate set.
- the three ingredients may be added separately into a blending assembly and mixed just ahead of a spray nozzle.
- the mixture is the immediately impelled as a homogeneous slurry into a mold or a target.
- the temperature of the mixture may be raised to further decrease the setting time (increase the speed of the reaction) or lowered to increase the setting time significantly (slow down the reaction).
- a third example of forming the mixture is forming the mixture over an endless belt to form various board and/or panel stocks.
- premanufactured insulation boards may be generated whereby a single board provides physical structure and, in addition, provides protection from heat and/or fire.
- wood chips can be added to the binder to manufacture fire retardant plywood or chipboard type boards.
- the subject method provides a family of nontoxic, fire resistive lightweight, low-cost, moldable, rigid insulations which satisfy the need the high speed, cost effective, energy efficient building construction technologies.
- the subject invention can be manufactured in a variety of ways, such as by continuous extrusion and endless belt production, as well as being sprayed from a blending device. Such methods of production depend on the ultimate shape and/or use of the product.
- the product has been tested in test buildings and has been found to be insulative at least up to 3000° F.
- the instant invention provides an effective fire protective and insulative barrier which further provides structural rigidity at a significantly decreased cost from prior art products and methods.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Nanotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Building Environments (AREA)
Abstract
A fire resistive and insulating bonded composite structure includes a binder made from a mixture of a weak acid and a powdered base metal oxide wherein the acid and metal fuse as a mixture under an exothermic reaction into the binder. A fibrous cellulose material is encapsulated within the binder and rendered non-flammable thereby. The subject invention further provides a method of making the bonded composite structure including the steps of mixing the weak acid and powdered base metal oxide, encapsulating the fibrous cellulose material within the binder and rendering the fibrous cellulose material non-flammable thereby, forming the slurry mixture into a predetermined form, and setting the formed mixture into a solid.
Description
This is a continuation of Ser. No. 832,323, filed Feb. 24, 1986, now abandoned.
This invention relates generally to bonded composite structures and methods for making the same. More particularly, this invention relates to bonded composite structures for forming fire resistive and insulating building materials and/or components such as panel structures, pipe insulation, and sprays for forming fire protective and insulating type coatings on pre-existing structures.
In the past, various materials have been used to form building materials such as molded panels. Initially, polyurethane and isocyanurate foamed plastics, both petroleum derivatives, were used to manufacture molded panels. Such panels were light weight, low cost, and thermally efficient. The components were readily available and could be easily transported. When the basic ingredients were combined, they expanded to approximately twenty times their original volume encapsulating myriads of minute gas bubbles. Initially, such panels were susceptible to slight shrinkage during set and cure stages. Such problems were later overcome. However, a controversy arose within the construction industry concerning the use of foam plastics in buildings. It was discovered that under certain conditions of heat and/or fire, the materials burned. The gases emitted were toxic. Under high heat with a spark, those gases could flash or explode. Additionally, since 1973, the subsequent ever upward spiraling cost of petroleum products further decreased the desirability of these foamed plastics as building components.
After a two year indepth analysis, it was determined by consent agreement between the Federal Trade Commission and the Society of Plastics Industry that foamed plastics could be used in buildings if they were totally encapsulated within fire resistive, nontoxic materials. Such materials were formed by encapsulating the foamed plastics in a variety of inorganic products such as a rigid homogenous foamed glass product manufactured by Pittsburgh Corning Corporation and marketed under the trademark "FOAMGLAS".
The U.S. Pat. No. 4,419,133 to Shubow et al, issued Dec. 6, 1983, discloses a bonded aggregate structure for making moldable rigid insulation. The Shubow et al patent discloses a bonded aggregate structure made from a mixture of magnesium oxide, aluminum oxide, aggregate, and mono aluminum phosphate acidic solution. The aggregates disclosed are cellular, low density aggregates selected from the group including inorganic materials such as glass beads, perlite, vermiculite, and stone or other refractory aggregates.
Further development has proceeded in search of methods of producing bonded composite structures at lower costs. Such structures must be of low cost but must also withstand high temperatures. The instant invention provides a low cost bonded composite structure wherein the binders are blended or mixed with a fibrous cellulose filler which is essentially a waste product that produces results similar to those achieved with the use of inorganic, insulating-type aggregates but at a much lower cost. Such organic materials would normally be highly flammable. Unexpectedly, however, pursuant to the subject invention, such cellulose filler materials do not burn and form rigid bonded structures able to withstand temperatures in excess of 3000° F.
The subject invention provides a bonded composite structure essentially consisting of a binder made from a mixture of a weak acid and a powdered base metal oxide, the acid and metal fusing as a mixture under an exothermic reaction into the binder. The invention is characterized by including a cellulose filler material encapsulated within the binder and rendered non-flammable thereby.
The subject invention further provides a method of making a bonded composite structure including the steps of mixing a weak acid and a powdered base metal oxide which fuse as a mixture under an exothermic reaction into a binder. A cellulose filler material is encapsulated within the binder and the cellulose filler material is rendered non-flammable thereby. The mixture is formed into a predetermined form and the formed mixture is set and cures to a solid structure.
The invention is a bonded composite structure consisting essentially of a binder material made from a mixture of a weak acid and a powdered base metal oxide and a cellulose filler material.
The reaction of the acid and base metal oxide form the binder which acts as a glue for encapsulating the cellulose filler material and for adhering the bonded composite structure to whatever surface the bonded composite structure is applied. In other words, the bonded composite structure is made by combining three or more ingredients in varying proportions depending upon the end product and time of set desired. The basic ingredients include a liquid not unlike the consistency of water, a powder not unlike the consistency of Portland cement, and a cellulose filler material.
The cellulose filler material can be selected from the group of cellulose waste materials including, but not limited to, saw dust, wood chips, shredded newspaper, straw, and bagasse. Other cellulose containing waste materials commonly discarded by the public may be utilized in the invention. The cost efficiency of these materials as compared to previously used inorganic aggregates is significant and thereby provides a distinct advantage to the subject invention. Such cellulose waste products are normally easily ignitable under normal conditions. Pursuant to the subject invention, however, the cellulose filler materials are encapsulated within the binder and rendered non-flammable thereby. While foamed plastic insulations (polystyrene, polyurenthane, isocyanrate and the like) can be fabricated into similar type products, they can melt at relatively low temperatures, they can burn, they can degrade under ultraviolet light, they can give off profuse amounts of smoke and toxic gases when ignited or, in some cases, only heated and, when utilized in habitable spaces, they must be enclosed or encapsulated within fire resistive materials. On the other hand, the subject invention will not begin to melt until temperatures in excess of 3000° F. have been reached. The subject invention will not burn. It will not degrade under ultraviolet light. It will not give off toxic gases, and it does not require a separate fire barrier. The subject invention is a fire barrier by itself. Moreover, while the foam plastic products are derivatives of petroleum and totally dependent upon the availability and price deviations of petroleum products, the subject invention is completely independent of the oil industry.
Preferably, the cellulose filler materials have a low density in the range from 3 to 15 pounds per cubic foot. Such low density materials are preferred in applications where high mass is a problem and low weight is desired.
The weak acid is selected from the group including mono aluminum phosphate. Other weak acids may be used which in combination with the powdered base metal oxide, such as magnesium oxide, form a magnesium phosphate solid. Such a magnesium phosphate solid will normally be formed relative quickly and stick to almost anything and binds together whatever materials might also happen to be in contact with the mixture. The weak acid and base metal oxide may be combined in a range of ratios from "3 to 1" to "1 to 3", respectively by weight. The cellulose filler materials are combined with the weak acid in a "1 to 1" to "1 to 6" ratio by weight.
The binder has a predetermined setting time. The binder can include water and/or other ingredient similar to those disclosed in the Shubow patent for delaying the setting time, the amount of water by part being directly related to the setting time. The set is chemical as when concrete or plaster mixes set. This is not a cure in the technical sense. Increasing the water content of the mixture can increase the setting time from an instantaneous to a 10 minute set.
Aluminum oxide can also be added to the mixture to increase the setting time. Increasing the relative proportion of aluminum oxide increases the setting time. The weight ratio of aluminum oxide to acidic solution is from about 1:1 to about 1:3 and the weight ratio of magnesium oxide to aluminum oxide is from about 1:1 to about 1:6.
Plasticizers can be used to adjust the plasticity of the final product without the further addition of water. Alternatively, plasticity can be kept constant by decreasing the amount of water in the mixture and adding a plasticizer. An example of a plasticizer is polypyrogenic silica having a particle size of 0.01 to 0.02 microns or the equivalent sold as X-59™ manufactured by Cabot Corporation, Boston, Mass.
The base metal can be magnesium oxide purchased from Martin Marietta Chemicals under the trade name MegChem. The base metal may include powder particles of a predetermined extent of being finally divided, the extent of being finally divided of the powder particles is directly related to the setting time. For example, the magnesium oxide may be purchased from Martin Marietta Chemicals as MagChem 40 or MagChem 30. MagChem 40 typically includes 98% magnesium oxide, has a particle size of 5 microns, and a surface area of 45 gm2. MagChem 30 is typically 98% magnesium oxide, has a particle size of 5 microns and a surface area of 20 gm2. The setting time for MagChem 30 is slower than the setting time for MagChem 40. This is attributed to MagChem 40 having more surface area.
The ammonium phosphate or aluminum phosphate may be purchased as ammonium phosphate or aluminum phosphate solution from Stauffer Chemical Company. Aluminum phosphate solution may also be referred to as aluminum phosphate or an acidic solution of mono aluminum phosphate. The ammonium phosphate or aluminum phosphate are a clear water white acidic aqueous solutions and are generally purchased as a 50% aqueous solutions.
The subject invention further provides a method of making the bonded composite structure. Generally, the method includes the steps of mixing the acid and the powdered base metal oxide which fuse as a mixture under an exothermic reaction into a binder. The fibrous cellulose material is encapsulated within the binder and is rendered non-flammable thereby. The mixture is formed into a predetermined form and the predetermined form is set during a predetermined period of time. The time for setting may be instantaneous or range up to or greater than 10 minutes. The setting time may be controlled by various factors set forth below. The setting time is chosen based on the desired end use of the encapsulated composite material.
For example, the mixture may be formed by extruding the mixture to form pipe insulation. In such an end use, water may be added to the mixture to delay the setting step for 30 second to 1 minute. Such alternation of the mixture provides what would be considered an intermediate setting time in comparison to the normally instantaneous setting time of the mixture. Alternatively, a less finally divided powdered metal oxide can be used to delay the setting step for 30 second to 1 minute.
The forming step may alternatively take the form of spraying the mixture onto a previously existing structure to form a fire protective and/or insulation layer on the structure. It is preferable in a spraying step to have material which almost instantaneously sets in 1 to 2 seconds. A blending approach, wherein the three ingredients are mixed together provides an almost immediate set. For example, the three ingredients may be added separately into a blending assembly and mixed just ahead of a spray nozzle. The mixture is the immediately impelled as a homogeneous slurry into a mold or a target. As temperature inversely affects the setting time of the mixture, the temperature of the mixture may be raised to further decrease the setting time (increase the speed of the reaction) or lowered to increase the setting time significantly (slow down the reaction).
A third example of forming the mixture is forming the mixture over an endless belt to form various board and/or panel stocks. In this manner, premanufactured insulation boards may be generated whereby a single board provides physical structure and, in addition, provides protection from heat and/or fire. For example, wood chips can be added to the binder to manufacture fire retardant plywood or chipboard type boards. By incorporating the cellulose waste materials, the cost of manufacturing and supplying such materials is significantly reduced.
The subject method provides a family of nontoxic, fire resistive lightweight, low-cost, moldable, rigid insulations which satisfy the need the high speed, cost effective, energy efficient building construction technologies. The subject invention can be manufactured in a variety of ways, such as by continuous extrusion and endless belt production, as well as being sprayed from a blending device. Such methods of production depend on the ultimate shape and/or use of the product. The product has been tested in test buildings and has been found to be insulative at least up to 3000° F. Thus, the instant invention provides an effective fire protective and insulative barrier which further provides structural rigidity at a significantly decreased cost from prior art products and methods.
The invention has been described in an illustrative manner, and it is to be understood that the terminology which has been used is intended to be in the nature of words of description rather than of limitation.
Obviously, many modifications and variations of the present invention are possible in light of the above teachings. It is, therefore, to be understood that with the scope of the appended claims the invention may be practiced otherwise than as specifically described.
TABLE 1
______________________________________
Brick No.
Sawdust Water MgO AlPO.sub.4
Plasticizer
______________________________________
1 1 0.3 2 3
2 1 1 2 2.5
3 1 1 2 2
4 1 1.5 2.25 2.25 0.35
______________________________________
Bricks were made by varying the ratios of ingredients as parts by weight as detailed in Table 1. The brinks had excellent heat resistant characteristics and were subjected to flames exceeding 3000° F.
TABLE 2 ______________________________________ Brick No. H.sub.2 O Acid Setting Time (seconds) ______________________________________ 1 20 80 20 2 30 70 25 3 50 50 25 ______________________________________
Bricks were made by varying the ratio of water to acid AlPO4 as parts by weight as detailed in Table 2. An increase in percent water by parts increased the setting time.
TABLE 3
______________________________________
Brick No.
Acid Water MgO Setting Time (seconds)
______________________________________
1 50 50 100 65
2 50 40 100 55
3 50 50 120 50
4 40 60 100 60
______________________________________
Bricks were made varying the ratios of acid (AlPO4), water and MgO as parts by weight and setting times were determined as detailed in Table 3. A decrease in water, keeping the acid and MgO constant, decreased the setting time. Decreasing the amount of MgO, keeping the amount of water and acid constant, increased the setting time.
TABLE 4 ______________________________________ Brick No. Straw Water MgO Acid ______________________________________ 1 1 1.5 2 2 2 1 1.5 2.5 21/2 3 1 1.5 3 3 4 1 1.5 5 5 ______________________________________
Bricks were made including the ingredients listed in Table 4 by weight. The bricks withstood exposure to flames exceeding 3000° F.
Claims (18)
1. A bonded composite structure consisting essentially of: a binder made from a mixture of mono aluminum phosphate and a powdered base metal oxide at a ratio of 3:1 to 1:3 by weight of powdered base metal oxide to weak acid, said acid and metal fusing as a mixture under an exothermic reaction into said binder without releasing any noxious gases, and intact fibrous cellulose material particles mixed throughout said binder at a ratio of 1:1 to 1:6 of said fibrous material to said weak acid and encapsulated within said binder and rendered non-flammable thereby in a single essentially homogeneous layer, said structure having a melting temperature greater than 3000° F.
2. A structure as set forth in claim 1 wherein said fibrous cellulose material is selected from the group of cellulose waste materials consisting of sawdust, wood chips, shredded newspaper, straw, and bagasse.
3. A bonded composite structure consisting essentially of: a binder made from a mixture of a weak acid selected from the group consisting of ammonium polyphosphate and mono aluminum phosphate and a powdered base metal oxide, said acid and metal fusing as a mixture under an exothermic reaction into said binder, and fibrous cellulose material particles encapsulated within said binder and rendered non-flammable thereby, said fibrous cellulose material having a low density in the range from 3 to 15 pounds per cubic foot.
4. A structure as set forth in claim 1 wherein said powdered base metal oxide being magnesium oxide and said weak acid and base metal oxide being combined in a 3:1 to 1:3 ratio by weight.
5. A structure as set forth in claim 4 wherein said fibrous cellulose material is combined with said weak acid in a 1:1 to 1:6 ratio by weight.
6. A structure as set forth in claim 1 wherein said binder has a predetermined setting time, said binder mixture including water for delaying said setting time of said binder, said amount of water by part being directly related to said setting time.
7. A structure as set forth in claim 1 wherein said base metal oxide includes powder particles of a predetermined extent of being finely divided, said extent of being finely divided of said powder particles being directly related to said setting time.
8. A structure as set forth in claim 1 including a plasticizer for increasing the plasticity of said mixture.
9. A method of making a bonded composite structure consisting essentially of the steps of: mixing mono aluminum phosphate and a powdered base metal oxide which fuse as a mixture under an exothermic reaction into a binder; mixing fibrous intact cellulose particles into the binder to suspend the fibrous cellulose particles throughout the binder while encapsulating the fibrous cellulose particles within the binder and rendering the fibrous cellulose particles non-flammable thereby; forming the mixture into a substantially homogenous layer of intact fibrous particles encapsulated in the binder; and setting the formed mixture.
10. A method as set forth in claim 9 wherein said forming step is further defined as extruding the mixture.
11. A method as set forth in claim 9 wherein said forming step is further defined as spraying said mixture onto a previously formed structure to form fire protective and/or an insulation layer on the structure.
12. A method as set forth in claim 11 wherein said setting step is further defined as instantaneously setting said mixture in one to two seconds.
13. A method as set forth in claim 9 wherein said forming step is further defined as forming the mixture on an endless belt to form board and/or panel stock.
14. A method as set forth in claim 9 wherein said fibrous cellulose material is selected from the group of cellulose waste materials consisting of sawdust, wood chips, shredded newspaper, straw, and bagasse.
15. A method as set forth in claim 14 wherein said fibrous cellulose material has a low density in the range from 3 to 15 pounds per cubic foot.
16. A method as set forth in claim 9 wherein said fibrous cellulose material is combined with said weak acid in a 1:1 to 1:6 ratio by weight.
17. A method as set forth in claim 9 wherein said binder having a predetermined setting time, said binder mixture including water for delaying said setting time of said binder, said amount of water by part being inversely related to said setting time.
18. A method as set forth in claim 9 wherein said base metal oxide including powder particles of a predetermined extent of being finely divided, said method further including the step of varying the size of the powder particles, said extent of being finely divided of said powder particles being directly related to said setting time.
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| Application Number | Priority Date | Filing Date | Title |
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| US07/110,615 US4981518A (en) | 1986-02-24 | 1987-10-19 | Bonded composite structure and method of making |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83232386A | 1986-02-24 | 1986-02-24 | |
| US07/110,615 US4981518A (en) | 1986-02-24 | 1987-10-19 | Bonded composite structure and method of making |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US83232386A Continuation | 1986-02-24 | 1986-02-24 |
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| Publication Number | Publication Date |
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| US4981518A true US4981518A (en) | 1991-01-01 |
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| Application Number | Title | Priority Date | Filing Date |
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| US07/110,615 Expired - Fee Related US4981518A (en) | 1986-02-24 | 1987-10-19 | Bonded composite structure and method of making |
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| US6235347B1 (en) | 1997-04-25 | 2001-05-22 | Astaris Llc | Fire resistant cellulosic materials and rendering such cellulosic materials leach resistant |
| US6395113B2 (en) * | 1996-02-23 | 2002-05-28 | Thermax Brandschutzbauteile Gmbh | Process for producing a non-combustible moulded article, especially a building panel |
| US6737115B2 (en) | 2002-06-03 | 2004-05-18 | Knight-Celotex, Llc | Method to reinforce cellulosic fiberboard panels via reinforcing bands on expansive surface |
| US20050060807A1 (en) * | 2003-09-19 | 2005-03-24 | Kazutoshi Kaizuka | Health pillow |
| WO2005047599A3 (en) * | 2003-11-08 | 2005-07-28 | Thomas J Lally | Method for manufacturing fire-retardant cellulose-based materials |
| WO2007028621A3 (en) * | 2005-09-07 | 2007-06-21 | Ks Aluminium Technologie Ag | Coating of a functional component that is subject to thermal loads and erosion, mold-release agent and method for producing said coating |
| WO2007075464A1 (en) * | 2005-12-16 | 2007-07-05 | 21St Century Structures, Llc | Inorganic composite material and manufacturing process |
| US20100212611A1 (en) * | 2007-11-02 | 2010-08-26 | Toyota Jidosha Kabushiki Kaisha | Internal combustion engine |
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| US20100304129A1 (en) * | 2005-09-07 | 2010-12-02 | Ks Aluminium-Technologie Ag | Coating of a functional component that is subject to thermal loads and erosion, mold-release agent and method for producing said coating |
| GB2446749A (en) * | 2005-12-16 | 2008-08-20 | 21St Century Structures Llc | inorganic composite material and manufacturing process |
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| WO2007075464A1 (en) * | 2005-12-16 | 2007-07-05 | 21St Century Structures, Llc | Inorganic composite material and manufacturing process |
| US20100212611A1 (en) * | 2007-11-02 | 2010-08-26 | Toyota Jidosha Kabushiki Kaisha | Internal combustion engine |
| WO2011100288A3 (en) * | 2010-02-09 | 2011-12-01 | Latitude 18, Inc. | Phosphate bonded composites and methods |
| CN102803177A (en) * | 2010-02-09 | 2012-11-28 | 18纬度有限公司 | Phosphate bonded composites and methods |
| US8425717B2 (en) | 2010-02-09 | 2013-04-23 | Latitude 18, Inc. | Phosphate bonded composites and methods |
| JP2013518806A (en) * | 2010-02-09 | 2013-05-23 | ラティテュード・18,インコーポレイテッド | Phosphate bonded composites and methods |
| US8603231B2 (en) | 2010-02-09 | 2013-12-10 | Latitude 18, Inc. | Phosphate bonded composites and methods |
| EP2534110A4 (en) * | 2010-02-09 | 2014-03-26 | Latitude 18 Inc | Phosphate bonded composites and methods |
| AU2011215966B2 (en) * | 2010-02-09 | 2016-02-18 | Latitude 18, Inc. | Phosphate bonded composites and methods |
| US20120110945A1 (en) * | 2010-11-10 | 2012-05-10 | Henry Hoang | Composites and Methods of Formation Thereof |
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